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De Bakker et al. Towards a 3 dimensional atlas of the developing hu, Prog Histochem Cytochem Jan 2013
 
Chieco et al. Image cytometry protocols for 2d and 3d quantific, Prog Histochem Cytochem Jan 2013
 
Cordell et al. Genome-wide association study identifies loci on 1, Human Molecular Genetics Jan 2013
 
Anderson et al. Recent developmental findings relevant to the clin, J Cardiovasc Electrophysiol Dec 2012
 
Anderson et al. Insights from cardiac development relevant to cong, J Cardiovasc Transl Res Dec 2012
 
Bornigen et al. An unbiased evaluation of gene prioritization tool, Bioinformatics Dec 2012
 
Yang et al. Inhibition of notch2 by numb numblike controls myo, Cardiovascular Research Nov 2012
 
Watanabe et al. Fibroblast growth factor 10 gene regulation in the, Proc Natl Acad Sci U S A Nov 2012
 
de Boer et al. Measurement and 3d-visualization of cell-cycle len, PLoS ONE Oct 2012
 
Lacucci et al. Reliance a machine learning and literature based , BMC Bioinformatics Sep 2012
 
Soemedi et al. Contribution of global rare copy number variants t, American Journal of Human Genetics Sep 2012
 
Sifrim et al. Annotate it a swiss knife approach to annotation, Genome Med Sep 2012
 
de Boer et al. Growth of the developing mouse heart an interacti, Developmental Biology Aug 2012
 
Blue et al. Congenital heart disease current knowledge about , Med J Aust Aug 2012
 
Louw et al. Haploinsufficiency of elastin gene may lead to fam, Am J Med Genet A Aug 2012
 
Kleefstra et al. Disruption of an ehmt1associated chromatin modifi, Am J Hum Genet Jul 2012
 
Moreau et al. Computational tools for prioritizing candidate gen, Nat Rev Genet Jul 2012
 
Fassbender et al. Combined mrna microarray and proteomic analysis of, Human Reproduction Jul 2012
 
Moradi Marjaneh et al. Qtl mapping of complex binary traits in advanced, Animal Genetics Jul 2012
 
Anderson et al. Normal and abnormal development of the intraperica, Cardiovasc Res Jul 2012
 
Howey et al. Premim and emim tools for estimation of maternal, BMC Bioinformatics Jun 2012
 
French et al. Nphp4 variants are associated with pleiotropic hea, Circ Res Jun 2012
 
Yu et al. Inhibition of notch2 by numb numblike controls myo, IEEE Transations on Pattern Analysis and Machine I May 2012
 
Yu et al. Kernel-based data fusion for machine learning, Studies in Computational Intelligence Springer May 2012
 
Koss et al. Congenital asplenia in mice and humans with mutati, Developmental Cell May 2012
 
Soemedi et al. Phenotype specific effect of chromosome 1q21 1 rea, Human Molecular Genetics Apr 2012
 
Sizarov et al. Three-dimensional and molecular analysis of the ar, J Anat Apr 2012
 
Breckpot et al. Congenital heart defects in a novel recurrent 22q1, Am J Med Genet A Mar 2012
 
de Bruyn et al. Hydrops fetalis and pulmonary lymphangiectasia due, Eur J Pediatr Mar 2012
 
Grandos Riveron et al. Combined mutation screening of nkx2-5 gata4 and t, Congenital Heart Disease Mar 2012
 
Konings et al. Microarray analysis of copy number variation in si, Nature Protocols Jan 2012
 
Breckpot et al. Bmpr1a is a candidate gene for congenital heart de, Eur J Med Genet Jan 2012
 
Breckpot et al. Differences in copy number variation between disco, Mol Syndromol Jan 2012
 
Guo et al. Genotype and cardiovascular phenotype correlations, Hum Mutat Nov 2011
 
Vermeesch et al. The causality of de novo copy number variants is o, Eur J Hum Genet Nov 2011
 
Esposito et al. Somatic mutations in nkx2-5 gata4 and hand1 are n, American Journal of Medical Genetics Oct 2011
 
Breckpot et al. Challenges of interpreting copy number variation i, Cytogenet Genome Res Sep 2011
 
Costa et al. Complex sumo-1 regulation of cardiac transcription, PLoS One Sep 2011
 
Sizarov et al. Molecular analysis of patterning of conduction tis, Circ Arrhythmia Elec Aug 2011
 
Bassett et al. Practical guidelines for managing patients with 22, J Pediatr Aug 2011
 
Cheng et al. Single-cell copy number variation detection, Genome Biology Aug 2011
 
Lacucci et al. Predicting receptor ligand pairs through kernel l, BMC Bioinformatics Aug 2011
 
Sizarov et al. Molecular analysis of patterning of conduction tis, Circ Arrhythm Electrophysiol Aug 2011
 
Van den Berg et al. Development of the pulmonary vein and the systemic, PLos ONE Jul 2011
 
Nitsch et al. Pinta a web server for network based gene priori, Nucleic Acids Research Web Server Issue Jul 2011
 
Qian et al. Tinmannkx2-5 acts via mir-1 and upstream of cdc42, J Cell Biol Jun 2011
 
Vermeesch et al. The causality of de novo copy number variants is o, Eur J Hum Genet May 2011
 
Caprioli et al. Nkx2-5 represses gatal gene expression and modulat, Circulation Apr 2011
 
Caprioli et al. Nkx2-5 represses gata1 gene expression and modulat, Circulation Apr 2011
 
Bondue et al. Defining the earliest step of cardiovascular proge, J Cell Biol Mar 2011
 
Sizarov et al. Formation of the building plan of the human heart , Circulation Mar 2011
 
Sizarov et al. Formation of the building plan of the human heart, Circulation Mar 2011
 
Bondue et al. Defining the earliest step of cardiovascular proge, Journal of Cell Biology Mar 2011
 
Lopes Floro et al. Loss of cited2 causes congenital heart disease by , Human Molecular Genetics Mar 2011
 
Takeuchi et al. Chromatin remodelling complex dosage modulates tra, Nature Communications Feb 2011
 
Paulussen et al. Mll2 mutation spectrum in 45 patients with kabuki , Hum Mutat Feb 2011
 
Takeuchi et al. Chromatin remodelling complex dosage modulates tra, Nat Commun Feb 2011
 
De Boer et al. The interactive presentation of 3d information obt, Development Jan 2011
 
de Boer et al. The interactive presentation of 3d information obt, Development Jan 2011
 
Ainsworth et al. Investigation of maternal effects, Genet Epidemiol Jan 2011
 
Furtado et al. Characterization of pitx2c expression in the mouse, Developmental Dynamics Jan 2011
 
Medioni et al. Expression of slit and robo genes in the developin, Developmental Dynamics Dec 2010
 
Breckpot et al. Duplication of the tgfbr1 gene causes features of , Eur J Med Genet Nov 2010
 
Brohee et al. Ytpdb a wiki database of yeast membrane transport, Biochim Biophys Acta Oct 2010
 
Schwinger et al. Clinical utility gene card for digeorge syndrome, Eur J Hum Genet Sep 2010
 
Brohee et al. Biological knowledge bases using wikis, Bioinformatics Sep 2010
 
Lai et al. Neuregulin 1 sustains the gene regulatory network , Circ Res Sep 2010
 
Thienpont et al. Haploinsufficiency of tab2 causes congenital heart, Am J Hum Genet Jun 2010
 
Breckpot et al. Array comparative genomic hybridization as a diagn, J Pedriatrics May 2010
 
Yuasa et al. Zac1 is an essential transcription factor for card, Circ Res Apr 2010
 
Posch et al. A gain-of-function tbx20 mutation causes human con, J Med Genet Apr 2010
 
Barriot et al. Collaboratively charting the gene-to-phenotype net, Genome Med Mar 2010
 
Thienpont et al. Duplications of the critical rubinstein-taybi dele, J Med Genet Mar 2010
 
De Boer et al. More than a decade of developmental gene expressio, Nuc Acid Res Dec 2009
 
Randall et al. Great vessel development requires biallelic expres, J Clin Invest Nov 2009
 
Xaymardan et al. C-kit function is necessary for in vitro myogenic, Stem Cells Aug 2009
 
Esposito et al. Molecular analysis of prkag2 lamp2 and nkx2-5 gen, Am J Med Genet Jul 2009
 
Macindoe et al. Conformational stability and dna binding specifici, J Mol Biol Jun 2009
 
Tomiyama et al. Phenotype of spontaneous orofacial dyskinesia, Progr Neurophysopharmacol Biol Psychiatry Mar 2009
 
Ferdous et al. Nkx2-5 transactivates the ets-related protein 71 g, Proc Natl Acad Sc Jan 2009